KIF18A

kinesin family member 18A

Summary

KIF18A is a member of the kinesin superfamily of microtubule-associated molecular motors (see MIM 148760) that use hydrolysis of ATP to produce force and movement along microtubules (Luboshits and Benayahu, 2005 [PubMed 15878648]).[supplied by OMIM, Aug 2008]

Known Variants47 total

rsidPosition (GRCh37)AllelesClassClinVar
rs132076559711:28,042,788T/Cuncertain significance
rs75154800911:28,042,796C/Tlikely benign
rs13997232611:28,042,799G/Aconflicting classifications of pathogenicity
rs19951261311:28,045,363T/Guncertain significance
rs3544065711:28,045,367G/Alikely benign
rs57645118111:28,049,720C/T
rs147698759111:28,057,803T/Auncertain significance
rs76477940011:28,057,844T/Cuncertain significance
rs213349638811:28,057,870C/Tuncertain significance
rs249426226911:28,057,882C/Tuncertain significance
rs249426258111:28,057,947T/Auncertain significance
rs14265684211:28,057,992A/Guncertain significance
rs15018487011:28,058,010G/Auncertain significance
rs249426293111:28,058,034T/Cuncertain significance
rs13874181011:28,058,043G/Auncertain significance
rs14937184711:28,058,052A/Guncertain significance
rs54613705111:28,058,058T/Cuncertain significance
rs120114880911:28,058,121T/Cuncertain significance
rs77597037911:28,058,144C/Tuncertain significance
rs748265011:28,074,833T/Gupstream gene variant
rs249429865211:28,080,486C/Guncertain significance
rs95322660211:28,080,535A/Glikely benign
rs18370094211:28,080,626A/Tuncertain significance
rs249429919311:28,080,641T/Guncertain significance
rs249429927811:28,080,670T/Cuncertain significance
rs185086836111:28,084,027G/Auncertain significance
rs37361950411:28,090,816T/Cuncertain significance
rs123410907411:28,090,820C/Tuncertain significance
rs76779875511:28,090,909T/Cuncertain significance
rs76574847111:28,090,927C/Tuncertain significance
rs249432771711:28,098,555T/Guncertain significance
rs77737150911:28,104,769C/Tuncertain significance
rs37613972011:28,106,212C/Guncertain significance
rs249433985211:28,106,243A/Guncertain significance
rs77994667111:28,106,273A/Guncertain significance
rs37567095211:28,110,163C/Tlikely benign
rs77189152111:28,110,165G/Cuncertain significance
rs76666279211:28,110,220G/Auncertain significance
rs132805560711:28,112,214G/Auncertain significance
rs37341528611:28,113,026T/Cuncertain significance
rs75825841211:28,116,210T/Cuncertain significance
rs117461947511:28,116,217T/Cuncertain significance
rs76247389311:28,119,206T/Cuncertain significance
rs75747420711:28,119,253T/Guncertain significance
rs75053878711:28,119,281G/Auncertain significance
rs74803128211:28,119,297C/Guncertain significance
rs185139701311:28,119,485T/Guncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.